Polymicrogyria

Known as: Polymicrogyria [Disease/Finding], Cerebral Polymicrogyrias, Polymicrogyria, Cerebral 
Heterogeneous disorders of cortical malformation characterized by excessive and small fused gyri and shallow sulci of the CORTEX with abnormal… (More)
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
Polymicrogyria is one of the most common malformations of cortical development and is associated with a variety of clinical… (More)
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Highly Cited
2010
Highly Cited
2010
The development of the human cerebral cortex is an orchestrated process involving the generation of neural progenitors in the… (More)
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Highly Cited
2009
Highly Cited
2009
Polymicrogyria is a relatively common but poorly understood defect of cortical development characterized by numerous small gyri… (More)
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Highly Cited
2007
Highly Cited
2007
Neural progenitor proliferation and migration influence brain size during neurogenesis. We report an autosomal recessive… (More)
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Highly Cited
2005
Highly Cited
2005
Human cerebral cortical polymicrogyria is a heterogeneous disorder, with only one known gene (GPR56) associated with an… (More)
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Highly Cited
2004
Highly Cited
2004
Joubert syndrome (JS) is an autosomal recessive disorder marked by agenesis of the cerebellar vermis, ataxia, hypotonia… (More)
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Highly Cited
2003
Highly Cited
2003
Identification of genes involved in human cerebral development is important for our understanding of disorders with potential… (More)
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2002
2002
BACKGROUND Subtle disorders of neuronal migration occur in the brains of some dyslexic patients who presented developmental… (More)
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1997
1997
We describe 9 patients with a bilateral malformation of cortical development, centered around the parasagittal and mesial aspects… (More)
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1984
1984
The cytoarchitectonics of the cerebral unlayered polymicrogyria located at the borders of a bilateral porencephalic defect is… (More)
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